US20030144677A1 - Reciprocating cutting and dilating balloon - Google Patents
Reciprocating cutting and dilating balloon Download PDFInfo
- Publication number
- US20030144677A1 US20030144677A1 US10/330,926 US33092602A US2003144677A1 US 20030144677 A1 US20030144677 A1 US 20030144677A1 US 33092602 A US33092602 A US 33092602A US 2003144677 A1 US2003144677 A1 US 2003144677A1
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- United States
- Prior art keywords
- balloon
- incising
- blade
- recited
- distal end
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 230000000916 dilatatory effect Effects 0.000 title description 4
- 208000031481 Pathologic Constriction Diseases 0.000 claims abstract description 59
- 208000037804 stenosis Diseases 0.000 claims abstract description 57
- 230000036262 stenosis Effects 0.000 claims abstract description 57
- 230000002792 vascular Effects 0.000 claims abstract description 24
- 210000005166 vasculature Anatomy 0.000 claims description 11
- 238000000034 method Methods 0.000 claims description 9
- 239000012530 fluid Substances 0.000 claims description 3
- 210000001367 artery Anatomy 0.000 description 8
- 230000010339 dilation Effects 0.000 description 8
- 230000008901 benefit Effects 0.000 description 2
- HVYWMOMLDIMFJA-DPAQBDIFSA-N cholesterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2 HVYWMOMLDIMFJA-DPAQBDIFSA-N 0.000 description 2
- 230000003176 fibrotic effect Effects 0.000 description 2
- 230000002093 peripheral effect Effects 0.000 description 2
- 208000037803 restenosis Diseases 0.000 description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 201000000057 Coronary Stenosis Diseases 0.000 description 1
- 206010011089 Coronary artery stenosis Diseases 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 230000001154 acute effect Effects 0.000 description 1
- 238000002399 angioplasty Methods 0.000 description 1
- 230000017531 blood circulation Effects 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 235000012000 cholesterol Nutrition 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 210000004351 coronary vessel Anatomy 0.000 description 1
- 210000001105 femoral artery Anatomy 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 230000037361 pathway Effects 0.000 description 1
Images
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B17/00—Surgical instruments, devices or methods
- A61B17/32—Surgical cutting instruments
- A61B17/3205—Excision instruments
- A61B17/3207—Atherectomy devices working by cutting or abrading; Similar devices specially adapted for non-vascular obstructions
- A61B17/320725—Atherectomy devices working by cutting or abrading; Similar devices specially adapted for non-vascular obstructions with radially expandable cutting or abrading elements
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B17/00—Surgical instruments, devices or methods
- A61B17/22—Implements for squeezing-off ulcers or the like on inner organs of the body; Implements for scraping-out cavities of body organs, e.g. bones; for invasive removal or destruction of calculus using mechanical vibrations; for removing obstructions in blood vessels, not otherwise provided for
- A61B2017/22038—Implements for squeezing-off ulcers or the like on inner organs of the body; Implements for scraping-out cavities of body organs, e.g. bones; for invasive removal or destruction of calculus using mechanical vibrations; for removing obstructions in blood vessels, not otherwise provided for with a guide wire
- A61B2017/22045—Implements for squeezing-off ulcers or the like on inner organs of the body; Implements for scraping-out cavities of body organs, e.g. bones; for invasive removal or destruction of calculus using mechanical vibrations; for removing obstructions in blood vessels, not otherwise provided for with a guide wire fixed to the catheter; guiding tip
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B17/00—Surgical instruments, devices or methods
- A61B17/22—Implements for squeezing-off ulcers or the like on inner organs of the body; Implements for scraping-out cavities of body organs, e.g. bones; for invasive removal or destruction of calculus using mechanical vibrations; for removing obstructions in blood vessels, not otherwise provided for
- A61B2017/22051—Implements for squeezing-off ulcers or the like on inner organs of the body; Implements for scraping-out cavities of body organs, e.g. bones; for invasive removal or destruction of calculus using mechanical vibrations; for removing obstructions in blood vessels, not otherwise provided for with an inflatable part, e.g. balloon, for positioning, blocking, or immobilisation
- A61B2017/22061—Implements for squeezing-off ulcers or the like on inner organs of the body; Implements for scraping-out cavities of body organs, e.g. bones; for invasive removal or destruction of calculus using mechanical vibrations; for removing obstructions in blood vessels, not otherwise provided for with an inflatable part, e.g. balloon, for positioning, blocking, or immobilisation for spreading elements apart
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M25/00—Catheters; Hollow probes
- A61M25/10—Balloon catheters
- A61M25/1002—Balloon catheters characterised by balloon shape
Definitions
- the present invention relates generally to surgical instruments. More particularly, the present invention pertains to surgical instruments for removing an obstruction in, or for enlarging the orifice of a vascular conduit or connective duct.
- the present invention is particularly, though not exclusively, useful for incising a stenosis within a vascular conduit and subsequently dilating the incised stenosis to increase bloodflow through the conduit.
- Coronary artery stenosis is primarily due to deposits of cholesterol, calcium and fibrotic tissue.
- the fibrotic tissue is usually the dominate of the three components and is a tightly composed matrix that, when incised, maintains its integrity on each side of the incision.
- Dilation of stenoses using standard angioplasty balloons has enjoyed widespread acceptance in the treatment of stenoses, however, this treatment protocol suffers from a high rate of restenosis.
- the present invention is directed to an apparatus for incising and dilating a stenosis within a vascular conduit of a patient. More specifically, the present invention is directed to an apparatus for incising a stenosis with relatively short incising blades that, due to their small size, can be easily guided through the bends and curves of the narrow vascular conduits to the site of the stenosis.
- the apparatus includes an inflatable balloon that is attached to the distal end of a catheter.
- the catheter is elongated and defines a longitudinal axis in the direction of elongation.
- the balloon extends axially from a distal end to a proximal end and is formed with an external surface.
- the balloon includes a tapered section that can extend to the distal end of the balloon. More specifically, due to the tapered section, the balloon narrows in the distal direction toward the distal end of the balloon. Consequently, within the tapered section, the external surface of the balloon includes a first point radially distanced from the longitudinal axis at a relatively large distance d 1 and a second point, distal to the first point, that is radially distanced from the longitudinal axis at a relatively small distance d 2 (d 1 >d 2 ), when the balloon is inflated.
- the apparatus further includes one or more incising blades, with each incising blade having a proximal end and a distal end.
- Each blade is attached to the external surface of the balloon, extending outwardly from the external surface and terminating in a cutting edge. More specifically, each incising blade is attached to the tapered section of the balloon.
- each incising blade is oriented with the proximal end of the blade radially distanced from the longitudinal axis at a distance r 1 and the distal end of the incising blade radially distanced from the longitudinal axis at a distance r 2 , with r 1 >r 2 .
- the balloon can be inflated to deploy each incising blade into a position where the blade is at an angle relative to the longitudinal axis of the catheter.
- This cooperation of structure allows the incising blades to cut an incision into a stenosis during axial advancement of the inflated balloon.
- the balloon when inflated, includes a tapered section that is conically shaped.
- incising blades formed with substantially straight cutting edges are used.
- each incising blade is formed with a curved advancing edge at the distal end of the incising blade to allow the incising blade to contact and cut a stenosis over the entire range of balloon inflation pressures.
- a balloon having a non-conical tapered section is used.
- the external surface of the tapered section in this embodiment is shaped as a surface of revolution defined by the rotation of a curve about the longitudinal axis.
- incising blades having cutting edges that are continuously curved from the distal end of the blade to the proximal end of the blade can be used.
- the balloon can be shaped wherein a portion of the balloon extends to a greater radial distance than the blades, after the balloon has been inflated. More specifically, the tapered section can extend proximally from the proximal end of each blade. With this cooperation of structure, there will be at least one point on the balloon that is distanced from the longitudinal axis at a distance d with d>r 1 after the balloon has been inflated. This cooperation of structure prevents the blades from cutting into or through the wall of the vascular conduit, while allowing the blades to incise a stenosis that protrudes from the wall of the vascular conduit and into the lumen of the vascular conduit.
- the catheter can include a flexible coil.
- the flexible coil is positioned proximal to the balloon.
- the balloon is formed with a cylindrical section that is positioned proximal to the tapered section with at least a portion of the flexible coil positioned inside the balloon.
- the flexible coil provides lateral flexibility to the apparatus, allowing the blades and at least a portion of the balloon to deflect from the proximal portion of the apparatus during advancement and withdrawal of the apparatus through the vascular conduits.
- the flexible coil provides good axial stiffness allowing the catheter to be pushed through the vascular conduits. Additionally, the coil is capable of transmitting the axial force required to push the incising blades through a stenosis during an incision.
- the balloon is first deflated, allowing each blade to assume. a position adjacent and parallel to the longitudinal axis.
- each blade is further positioned between adjacent balloon folds to prevent exposure of the cutting edges to the walls of the vascular conduits while the apparatus is navigated through the vascular conduits of the patient.
- the distal end of the apparatus is inserted into a vascular conduit such as a peripheral artery and advanced through the vasculature until the blades and balloon are positioned in front of a stenosis.
- a guidewire can be used to establish a mechanical pathway to assist the distal end of the apparatus to the site of the stenosis.
- the balloon is at least partially inflated causing the balloon and incising blades to move outwardly together in a radial direction from the longitudinal axis.
- the proximal end of each blade moves a greater radial distance than the distal end of the blade during inflation, positioning the proximal end of each blade at a greater radial distance from the longitudinal axis than the distal end of each incision blade. It is to be appreciated that the proximal end of each blade can be moved to a selected radial distance by controlling the inflation pressure within the balloon.
- the apparatus can then be axially advanced to push one or more of the incising blades through the stenosis.
- the apparatus can be axially withdrawn until the blades are once again positioned in front of the stenosis.
- the inflation pressure can be adjusted to increase/decrease the radial distance between the longitudinal axis than the proximal end of each incision blade, and thus modify the incision depth.
- the apparatus can once again be axially advanced to push the incising blades through the stenosis. This process can then be repeated as many times as desired.
- the apparatus can be used to dilate the incised stenosis. Specifically, the apparatus can be axially advanced/withdrawn until a selected portion of the balloon, such as a portion of the balloon proximal to the tapered section, is positioned adjacent to the stenosis. In some cases, the balloon may need to be at least partially deflated (relative to the inflation pressure used for incising) to position the balloon for dilation. With the proximal portion of the balloon positioned adjacent the stenosis, the balloon can be expanded to dilate the incised stenosis. After the stenosis has been incised and dilated, the balloon can be deflated to thereby allow the apparatus to be moved for treatment of another stenosis or withdrawn from the patient's body.
- a selected portion of the balloon such as a portion of the balloon proximal to the tapered section
- the balloon may need to be at least partially deflated (relative to the inflation pressure used for inc
- FIG. 1 is a simplified, schematic view showing an apparatus in accordance with the present invention operationally positioned in a patient to incise and dilate a stenosis in an upper body artery;
- FIG. 2 is an enlarged perspective view of the distal portion of an apparatus in accordance with the present invention, shown after balloon inflation;
- FIG. 3 is an enlarged elevation view of the distal portion of an apparatus in accordance with the present invention, shown after balloon inflation;
- FIG. 4 is a cross-sectional view of the balloon and incising blades as seen along line 4 - 4 in FIG. 3;
- FIG. 5 is a cross-sectional view of the catheter showing the inflation/deflation tube as seen along line 5 - 5 in FIG. 3;
- FIG. 6A is an enlarged elevation view of the distal portion of another embodiment in accordance with the present invention having blades with curved cutting edges, shown with the balloon in the deflated configuration;
- FIG. 6B is a cross-sectional view along line 6 B- 6 B in FIG. 1 of the distal portion of the apparatus shown in FIG. 6A, shown after balloon inflation;
- FIG. 7 is schematic view of the distal portion of still another embodiment in accordance with the present invention having a balloon with a tapered section for deploying the incising blades and a cylindrical section for dilation;
- FIG. 8 is a schematic view of the apparatus shown in FIG. 8, shown positioned in a curved vascular conduit.
- an apparatus for incising and dilating a stenosis within a vascular conduit is shown and generally designated 10 . More specifically, the apparatus 10 is shown positioned for treatment of an upper body artery in a patient 12 . Although the apparatus 10 is capable of treating a stenosis in an upper body artery such as a coronary artery, those skilled in the pertinent art will recognize that the use of the apparatus 10 is not limited to upper body arteries, but, instead can be used in vascular conduits and other ductal systems throughout the human body, and is also suitable for use in plants and animals.
- the distal end of the apparatus 10 is shown to include an inflatable balloon 14 that is attached to the distal end 18 of an elongated tubular catheter 20 .
- the catheter 20 can include a flexible, helical coil 21 positioned proximal to the balloon 14 .
- the apparatus 10 includes incising blades 22 a - d that are attached to the external surface 24 of the balloon 14 and circumferentially distributed around the balloon 14 .
- the balloon 14 and catheter 20 (including the coil 21 ) are formed with a contiguous lumen to allow the balloon 14 and catheter 20 (including the coil 21 ) to travel over a guidewire 26 .
- the elongated catheter 20 defines a longitudinal axis 28 in the direction of elongation.
- the balloon 14 extends axially from a distal end 30 to a proximal end 32 , defining a length L that is typically in the range of approximately five to six millimeters (5-6 mm).
- the balloon 14 includes a tapered section 34 that extends to the distal end 30 of the balloon 14 . More specifically, within the tapered section 34 , the balloon 14 is conically shaped and narrows in the distal direction toward the distal end 30 of the balloon 14 .
- the inflated balloon 14 includes a first point radially distanced from the longitudinal axis 28 at a relatively large distance d 1 and a second point, distal to the first point, that is radially distanced from the longitudinal axis 28 at a relatively small distance d 2 (d 1 >d 2 ), as shown.
- each incising blade 22 extends from a proximal end 36 to a distal end 38 defining a length therebetween that is typically in the range of approximately two to four millimeters (2-4 mm). As shown, each incising blade 22 is positioned on the tapered section 34 of the balloon 14 . As best seen in FIG. 4, each blade 22 a - d is attached to the external surface 24 of the balloon 14 and extends outwardly from the external surface 24 to respective cutting edge 40 a - d . Referring back to FIG.
- each incising blade 22 is formed with a substantially straight cutting edge 40 having a curved advancing edge at the distal end 30 to allow the incising blade 22 to contact and cut a stenosis over the entire range of balloon 14 inflation pressures. It can be further seen that after the balloon 14 has been inflated, each incising blade 22 is oriented with the proximal end 36 of the blade 22 radially distanced from the longitudinal axis 28 at a distance r 1 and the distal end 38 of the incising blade 22 radially distanced from the longitudinal axis 28 at a distance r 2 , with r 1 >r 2 .
- the balloon 14 can be inflated to deploy each incising blade 22 into a position where the blade 22 is at an angle relative to the longitudinal axis 28 .
- This cooperation of structure allows the incising blades 22 to cut an incision into a stenosis during axial advancement of the inflated balloon 14 .
- the inflated balloon 14 is shaped wherein a portion of the balloon 14 extends to a greater radial distance from the longitudinal axis 28 than the proximal end 36 of each blade 22 .
- FIG. 3 shows that the tapered section 34 can extend proximally from the proximal end 36 of each blade 22 .
- an inflation tube 41 extends through the catheter 20 to allow for inflation/deflation of the balloon 14 from an extracorporeal location.
- the apparatus 110 includes a balloon 114 having a non-conical tapered section 134 attached to the distal end 118 of a catheter 120 that includes a flexible, helical coil 121 positioned proximal to the balloon 114 .
- the external surface 124 of the tapered section 134 is shaped as a surface of revolution defined by the rotation of a curve about the longitudinal axis 128 .
- incising blades 122 a - c have cutting edges 140 that are continuously curved from the distal end 138 to the proximal end 136 are used.
- the apparatus 210 includes a balloon 214 having tapered section 234 and a cylindrical dilation section 42 positioned proximal to the tapered section 234 .
- the balloon 214 is attached to the distal end 218 of a catheter 220 that includes a flexible, helical coil 221 .
- the coil 221 is positioned inside the balloon 214 .
- Incising blades 222 are mounted on the tapered section 234 of the balloon 214 .
- the catheter 220 including the helical coil 221 , establish a lumen to allow the catheter 220 , balloon 214 and blades 222 to travel over guidewire 226 .
- a guidewire such as guidewire 126 shown in FIGS. 6A and 6B, is inserted into the opening and advanced through the patient's vasculature.
- the guidewire 126 is advanced and steered into the vascular conduit 44 of interest and then advanced past the stenosis 46 requiring treatment.
- the balloon 114 is first collapsed into the deflated configuration as shown in FIG. 6A. As shown in FIG.
- each blade 122 a - c in the deflated configuration, is positioned adjacent and substantially parallel to the longitudinal axis 128 , allowing the apparatus 110 to fit into a small access opening and to more easily transit through the vasculature.
- the apparatus 110 is threaded onto the guidewire 126 at an extracorporeal location, inserted into the access opening and advanced over the guidewire 126 until the balloon 114 is positioned in the vascular conduit 44 of interest and in front of the stenosis 46 requiring treatment.
- the flexible coil 221 provides lateral flexibility to the apparatus 210 , allowing the blades 222 to deflect from the proximal portion of the apparatus 210 . This deflection allows the apparatus 210 to navigate through acute angles in a vascular conduit 47 , as shown in FIG. 8.
- the balloon 114 is inflated to deploy the incising blades 122 .
- inflation fluid from fluid source 48 can be passed under control of controller 50 through inflation tube 141 and into the balloon 114 . It is to be appreciated that the proximal end 136 of each blade 122 can be moved to a selected radial distance by controlling the inflation pressure within the balloon 114 .
- the apparatus 110 can then be axially advanced to push one or more of the incising blades 122 through the stenosis 46 . If required, a reciprocating force can be applied to the apparatus 110 from the periphery to pass the blades 122 through the stenosis 46 .
- the flexible coil 121 provides good axial stiffness, and thus effectively transmits the axial force necessary to incise the stenosis 46 .
- the apparatus 110 can be axially withdrawn until the blades 122 are once again positioned in front of the stenosis 46 .
- the inflation pressure can be adjusted to modify the incision depth.
- the apparatus 110 can once again be axially advanced to push the incising blades 122 through the stenosis 46 . This process can then be repeated as many times as desired.
- the apparatus 110 can be used to dilate the incised stenosis 46 .
- the apparatus 110 can be axially advanced until the largest diameter portion of the balloon (i.e. point 54 on balloon 114 ) passes through and dilates the stenosis 46 .
- the balloon 114 can be positioned with the largest diameter portion of the balloon (i.e. point 54 on balloon 114 ) within the stenosis 46 . Once positioned, the balloon 114 can be further distended to dilate the stenosis 46 .
- the cylindrical dilation section of the balloon 214 can be used to dilate a relatively long stenosis.
- the balloon 114 can be deflated to thereby allow the apparatus 110 to be moved for treatment of another stenosis or withdrawn from the patient's body.
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Abstract
Description
- This application claims the benefit of U.S. Provisional Application No. 60/351,893 filed Jan. 25, 2002, U.S. Provisional Application No. 60/356,273 filed Feb. 12, 2002 and U.S. Provisional Application No. 60/368,009 filed Mar. 27, 2002.
- The present invention relates generally to surgical instruments. More particularly, the present invention pertains to surgical instruments for removing an obstruction in, or for enlarging the orifice of a vascular conduit or connective duct. The present invention is particularly, though not exclusively, useful for incising a stenosis within a vascular conduit and subsequently dilating the incised stenosis to increase bloodflow through the conduit.
- Coronary artery stenosis is primarily due to deposits of cholesterol, calcium and fibrotic tissue. The fibrotic tissue is usually the dominate of the three components and is a tightly composed matrix that, when incised, maintains its integrity on each side of the incision. Dilation of stenoses using standard angioplasty balloons has enjoyed widespread acceptance in the treatment of stenoses, however, this treatment protocol suffers from a high rate of restenosis. Recent studies, however, indicate that restenosis can be prevented by first incising the material that is creating the stenosis followed by dilation of the incised stenosis. After incision, a stenosis is more easily flattened, and the likelihood of damaging the artery during dilation is reduced. In most applications, incision lengths of up to approximately fifteen millimeters (15 mm) are required, followed by dilation of the incised stenosis.
- The present invention is directed to an apparatus for incising and dilating a stenosis within a vascular conduit of a patient. More specifically, the present invention is directed to an apparatus for incising a stenosis with relatively short incising blades that, due to their small size, can be easily guided through the bends and curves of the narrow vascular conduits to the site of the stenosis. For the present invention, the apparatus includes an inflatable balloon that is attached to the distal end of a catheter. The catheter is elongated and defines a longitudinal axis in the direction of elongation. At the distal end of the catheter, the balloon extends axially from a distal end to a proximal end and is formed with an external surface. Also for the present invention, the balloon includes a tapered section that can extend to the distal end of the balloon. More specifically, due to the tapered section, the balloon narrows in the distal direction toward the distal end of the balloon. Consequently, within the tapered section, the external surface of the balloon includes a first point radially distanced from the longitudinal axis at a relatively large distance d1 and a second point, distal to the first point, that is radially distanced from the longitudinal axis at a relatively small distance d2 (d1>d2), when the balloon is inflated.
- In accordance with the present invention, the apparatus further includes one or more incising blades, with each incising blade having a proximal end and a distal end. Each blade is attached to the external surface of the balloon, extending outwardly from the external surface and terminating in a cutting edge. More specifically, each incising blade is attached to the tapered section of the balloon. For the present invention, each incising blade is oriented with the proximal end of the blade radially distanced from the longitudinal axis at a distance r1 and the distal end of the incising blade radially distanced from the longitudinal axis at a distance r2, with r1>r2. As a consequence, the balloon can be inflated to deploy each incising blade into a position where the blade is at an angle relative to the longitudinal axis of the catheter. This cooperation of structure allows the incising blades to cut an incision into a stenosis during axial advancement of the inflated balloon.
- In one embodiment of the present invention, the balloon, when inflated, includes a tapered section that is conically shaped. In this embodiment, incising blades formed with substantially straight cutting edges are used. However, for this embodiment, each incising blade is formed with a curved advancing edge at the distal end of the incising blade to allow the incising blade to contact and cut a stenosis over the entire range of balloon inflation pressures. In another embodiment of the present invention, a balloon having a non-conical tapered section is used. Specifically, the external surface of the tapered section in this embodiment is shaped as a surface of revolution defined by the rotation of a curve about the longitudinal axis. For this embodiment, incising blades having cutting edges that are continuously curved from the distal end of the blade to the proximal end of the blade can be used.
- In both the straight blade and curved blade embodiments, the balloon can be shaped wherein a portion of the balloon extends to a greater radial distance than the blades, after the balloon has been inflated. More specifically, the tapered section can extend proximally from the proximal end of each blade. With this cooperation of structure, there will be at least one point on the balloon that is distanced from the longitudinal axis at a distance d with d>r1 after the balloon has been inflated. This cooperation of structure prevents the blades from cutting into or through the wall of the vascular conduit, while allowing the blades to incise a stenosis that protrudes from the wall of the vascular conduit and into the lumen of the vascular conduit.
- To further allow the apparatus to be easily navigated through the vascular conduits of a patient, the catheter can include a flexible coil. In a particular embodiment of the present invention, the flexible coil is positioned proximal to the balloon. In another embodiment of the present invention, the balloon is formed with a cylindrical section that is positioned proximal to the tapered section with at least a portion of the flexible coil positioned inside the balloon. The flexible coil provides lateral flexibility to the apparatus, allowing the blades and at least a portion of the balloon to deflect from the proximal portion of the apparatus during advancement and withdrawal of the apparatus through the vascular conduits. On the other hand, the flexible coil provides good axial stiffness allowing the catheter to be pushed through the vascular conduits. Additionally, the coil is capable of transmitting the axial force required to push the incising blades through a stenosis during an incision.
- In operation, the balloon is first deflated, allowing each blade to assume. a position adjacent and parallel to the longitudinal axis. In a particular implementation, each blade is further positioned between adjacent balloon folds to prevent exposure of the cutting edges to the walls of the vascular conduits while the apparatus is navigated through the vascular conduits of the patient. With the balloon deflated, the distal end of the apparatus is inserted into a vascular conduit such as a peripheral artery and advanced through the vasculature until the blades and balloon are positioned in front of a stenosis. For this purpose, a guidewire can be used to establish a mechanical pathway to assist the distal end of the apparatus to the site of the stenosis. Next, the balloon is at least partially inflated causing the balloon and incising blades to move outwardly together in a radial direction from the longitudinal axis. In greater detail, the proximal end of each blade moves a greater radial distance than the distal end of the blade during inflation, positioning the proximal end of each blade at a greater radial distance from the longitudinal axis than the distal end of each incision blade. It is to be appreciated that the proximal end of each blade can be moved to a selected radial distance by controlling the inflation pressure within the balloon.
- With the blades deployed in this manner, the apparatus can then be axially advanced to push one or more of the incising blades through the stenosis. Next, if required, the apparatus can be axially withdrawn until the blades are once again positioned in front of the stenosis. At this point, the inflation pressure can be adjusted to increase/decrease the radial distance between the longitudinal axis than the proximal end of each incision blade, and thus modify the incision depth. With the blades adjusted for the proper incision depth, the apparatus can once again be axially advanced to push the incising blades through the stenosis. This process can then be repeated as many times as desired.
- Once the stenosis has been satisfactorily incised, the apparatus can be used to dilate the incised stenosis. Specifically, the apparatus can be axially advanced/withdrawn until a selected portion of the balloon, such as a portion of the balloon proximal to the tapered section, is positioned adjacent to the stenosis. In some cases, the balloon may need to be at least partially deflated (relative to the inflation pressure used for incising) to position the balloon for dilation. With the proximal portion of the balloon positioned adjacent the stenosis, the balloon can be expanded to dilate the incised stenosis. After the stenosis has been incised and dilated, the balloon can be deflated to thereby allow the apparatus to be moved for treatment of another stenosis or withdrawn from the patient's body.
- The novel features of this invention, as well as the invention itself, both as to its structure and its operation, will be best understood from the accompanying drawings, taken in conjunction with the accompanying description, in which similar reference characters refer to similar parts, and in which:
- FIG. 1 is a simplified, schematic view showing an apparatus in accordance with the present invention operationally positioned in a patient to incise and dilate a stenosis in an upper body artery;
- FIG. 2 is an enlarged perspective view of the distal portion of an apparatus in accordance with the present invention, shown after balloon inflation;
- FIG. 3 is an enlarged elevation view of the distal portion of an apparatus in accordance with the present invention, shown after balloon inflation;
- FIG. 4 is a cross-sectional view of the balloon and incising blades as seen along line4-4 in FIG. 3;
- FIG. 5 is a cross-sectional view of the catheter showing the inflation/deflation tube as seen along line5-5 in FIG. 3;
- FIG. 6A is an enlarged elevation view of the distal portion of another embodiment in accordance with the present invention having blades with curved cutting edges, shown with the balloon in the deflated configuration;
- FIG. 6B is a cross-sectional view along
line 6B-6B in FIG. 1 of the distal portion of the apparatus shown in FIG. 6A, shown after balloon inflation; - FIG. 7 is schematic view of the distal portion of still another embodiment in accordance with the present invention having a balloon with a tapered section for deploying the incising blades and a cylindrical section for dilation; and
- FIG. 8 is a schematic view of the apparatus shown in FIG. 8, shown positioned in a curved vascular conduit.
- Referring initially to FIG. 1, an apparatus for incising and dilating a stenosis within a vascular conduit is shown and generally designated10. More specifically, the
apparatus 10 is shown positioned for treatment of an upper body artery in apatient 12. Although theapparatus 10 is capable of treating a stenosis in an upper body artery such as a coronary artery, those skilled in the pertinent art will recognize that the use of theapparatus 10 is not limited to upper body arteries, but, instead can be used in vascular conduits and other ductal systems throughout the human body, and is also suitable for use in plants and animals. - Referring now to FIG. 2, the distal end of the
apparatus 10 is shown to include aninflatable balloon 14 that is attached to thedistal end 18 of an elongatedtubular catheter 20. As shown, thecatheter 20 can include a flexible,helical coil 21 positioned proximal to theballoon 14. As further shown in FIG. 2, theapparatus 10 includes incising blades 22 a-d that are attached to theexternal surface 24 of theballoon 14 and circumferentially distributed around theballoon 14. As further shown, theballoon 14 and catheter 20 (including the coil 21) are formed with a contiguous lumen to allow theballoon 14 and catheter 20 (including the coil 21) to travel over aguidewire 26. - Referring now to FIG. 3, it can be seen that the
elongated catheter 20 defines alongitudinal axis 28 in the direction of elongation. As further shown, theballoon 14 extends axially from adistal end 30 to aproximal end 32, defining a length L that is typically in the range of approximately five to six millimeters (5-6 mm). Also shown, theballoon 14 includes a taperedsection 34 that extends to thedistal end 30 of theballoon 14. More specifically, within the taperedsection 34, theballoon 14 is conically shaped and narrows in the distal direction toward thedistal end 30 of theballoon 14. Consequently, theinflated balloon 14 includes a first point radially distanced from thelongitudinal axis 28 at a relatively large distance d1 and a second point, distal to the first point, that is radially distanced from thelongitudinal axis 28 at a relatively small distance d2 (d1>d2), as shown. - With continued reference to FIG. 3, it can be seen that each incising blade22 extends from a
proximal end 36 to a distal end 38 defining a length therebetween that is typically in the range of approximately two to four millimeters (2-4 mm). As shown, each incising blade 22 is positioned on the taperedsection 34 of theballoon 14. As best seen in FIG. 4, each blade 22 a-d is attached to theexternal surface 24 of theballoon 14 and extends outwardly from theexternal surface 24 to respective cutting edge 40 a-d. Referring back to FIG. 3, it can be seen that each incising blade 22 is formed with a substantially straight cutting edge 40 having a curved advancing edge at thedistal end 30 to allow the incising blade 22 to contact and cut a stenosis over the entire range ofballoon 14 inflation pressures. It can be further seen that after theballoon 14 has been inflated, each incising blade 22 is oriented with theproximal end 36 of the blade 22 radially distanced from thelongitudinal axis 28 at a distance r1 and the distal end 38 of the incising blade 22 radially distanced from thelongitudinal axis 28 at a distance r2, with r1>r2. As a consequence of this orientation, theballoon 14 can be inflated to deploy each incising blade 22 into a position where the blade 22 is at an angle relative to thelongitudinal axis 28. This cooperation of structure allows the incising blades 22 to cut an incision into a stenosis during axial advancement of theinflated balloon 14. - Continuing with reference to FIG. 3, it can be seen that the
inflated balloon 14 is shaped wherein a portion of theballoon 14 extends to a greater radial distance from thelongitudinal axis 28 than theproximal end 36 of each blade 22. In greater detail, FIG. 3 shows that the taperedsection 34 can extend proximally from theproximal end 36 of each blade 22. With this cooperation of structure, there will be at least one point on theinflated balloon 14 that is distanced from thelongitudinal axis 28 at a distance greater than r1. This cooperation of structure prevents the blades 22 from cutting into or through the wall of the vascular conduit, while allowing the blades 22 to incise a stenosis that protrudes from the wall of the vascular conduit and into the lumen of the vascular conduit. With cross reference to FIGS. 3 and 5, it can be seen that aninflation tube 41 extends through thecatheter 20 to allow for inflation/deflation of theballoon 14 from an extracorporeal location. - Referring now to FIGS. 6A and 6B, another embodiment of the apparatus (labeled110) is shown. As further shown, the
apparatus 110 includes aballoon 114 having a non-conicaltapered section 134 attached to thedistal end 118 of acatheter 120 that includes a flexible,helical coil 121 positioned proximal to theballoon 114. It is to be appreciated from FIG. 6B, theexternal surface 124 of the taperedsection 134 is shaped as a surface of revolution defined by the rotation of a curve about the longitudinal axis 128. For this embodiment, incisingblades 122 a-c have cuttingedges 140 that are continuously curved from thedistal end 138 to theproximal end 136 are used. - Referring now to FIG. 7, another embodiment of the apparatus (labeled210) is shown. As further shown, the
apparatus 210 includes aballoon 214 having taperedsection 234 and acylindrical dilation section 42 positioned proximal to the taperedsection 234. It can be further seen that theballoon 214 is attached to thedistal end 218 of acatheter 220 that includes a flexible,helical coil 221. In this embodiment, as shown, thecoil 221 is positioned inside theballoon 214.Incising blades 222 are mounted on the taperedsection 234 of theballoon 214. It is to be appreciated that thecatheter 220, including thehelical coil 221, establish a lumen to allow thecatheter 220,balloon 214 andblades 222 to travel overguidewire 226. - To use the
apparatus guidewire 126 shown in FIGS. 6A and 6B, is inserted into the opening and advanced through the patient's vasculature. Theguidewire 126 is advanced and steered into thevascular conduit 44 of interest and then advanced past thestenosis 46 requiring treatment. With theguidewire 126 in place, theballoon 114 is first collapsed into the deflated configuration as shown in FIG. 6A. As shown in FIG. 6A, in the deflated configuration, eachblade 122 a-c is positioned adjacent and substantially parallel to the longitudinal axis 128, allowing theapparatus 110 to fit into a small access opening and to more easily transit through the vasculature. - Next, the
apparatus 110 is threaded onto theguidewire 126 at an extracorporeal location, inserted into the access opening and advanced over theguidewire 126 until theballoon 114 is positioned in thevascular conduit 44 of interest and in front of thestenosis 46 requiring treatment. During advancement of the apparatus (such asapparatus 210 shown in FIG. 8) through the vasculature, theflexible coil 221 provides lateral flexibility to theapparatus 210, allowing theblades 222 to deflect from the proximal portion of theapparatus 210. This deflection allows theapparatus 210 to navigate through acute angles in avascular conduit 47, as shown in FIG. 8. - Continuing now with cross reference to FIGS. 1 and 6A, once the
balloon 114 is positioned in front of thestenosis 46, theballoon 114 is inflated to deploy theincising blades 122. In greater detail, inflation fluid fromfluid source 48 can be passed under control ofcontroller 50 throughinflation tube 141 and into theballoon 114. It is to be appreciated that theproximal end 136 of eachblade 122 can be moved to a selected radial distance by controlling the inflation pressure within theballoon 114. - With the
blades 122 deployed in this manner, theapparatus 110 can then be axially advanced to push one or more of the incisingblades 122 through thestenosis 46. If required, a reciprocating force can be applied to theapparatus 110 from the periphery to pass theblades 122 through thestenosis 46. During advancement of theblades 122 through thestenosis 46, theflexible coil 121 provides good axial stiffness, and thus effectively transmits the axial force necessary to incise thestenosis 46. After initial incision, if desired, theapparatus 110 can be axially withdrawn until theblades 122 are once again positioned in front of thestenosis 46. At this point, the inflation pressure can be adjusted to modify the incision depth. With theblades 122 adjusted for the proper incision depth, theapparatus 110 can once again be axially advanced to push theincising blades 122 through thestenosis 46. This process can then be repeated as many times as desired. - Once the
stenosis 46 has been satisfactorily incised, theapparatus 110 can be used to dilate the incisedstenosis 46. Specifically, theapparatus 110 can be axially advanced until the largest diameter portion of the balloon (i.e.point 54 on balloon 114) passes through and dilates thestenosis 46. Alternatively, with theballoon 114 partially inflated, theballoon 114 can be positioned with the largest diameter portion of the balloon (i.e.point 54 on balloon 114) within thestenosis 46. Once positioned, theballoon 114 can be further distended to dilate thestenosis 46. When the embodiment shown in FIGS. 7 and 8 is used, the cylindrical dilation section of theballoon 214 can be used to dilate a relatively long stenosis. After the stenosis 46 (see FIG. 6B) has been incised and dilated, theballoon 114 can be deflated to thereby allow theapparatus 110 to be moved for treatment of another stenosis or withdrawn from the patient's body. - While the particular apparatus and methods as herein shown and disclosed in detail are fully capable of obtaining the objects and providing the advantages herein before stated, it is to be understood that they are merely illustrative of the presently preferred embodiments of the invention and that no limitations are intended to the details of construction or design herein shown other than as described in the appended claims.
Claims (20)
Priority Applications (8)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US10/330,926 US6951566B2 (en) | 2002-01-25 | 2002-12-27 | Reciprocating cutting and dilating balloon |
EP03814604A EP1581298B1 (en) | 2002-12-27 | 2003-10-14 | Reciprocating cutting and dilating balloon |
DE60307897T DE60307897T2 (en) | 2002-12-27 | 2003-10-14 | ROTATING CUTTING AND DILATATION BALLOON |
CA002511544A CA2511544A1 (en) | 2002-12-27 | 2003-10-14 | Reciprocating cutting and dilating balloon |
JP2004564786A JP2006512137A (en) | 2002-12-27 | 2003-10-14 | Reciprocal cutting / expansion balloon |
PCT/US2003/032465 WO2004060467A1 (en) | 2002-12-27 | 2003-10-14 | Reciprocating cutting and dilating balloon |
AU2003303621A AU2003303621A1 (en) | 2002-12-27 | 2003-10-14 | Reciprocating cutting and dilating balloon |
AT03814604T ATE337044T1 (en) | 2002-12-27 | 2003-10-14 | REciprocating CUTTING AND DILATION BALLOON |
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
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US35189302P | 2002-01-25 | 2002-01-25 | |
US35627302P | 2002-02-12 | 2002-02-12 | |
US36800902P | 2002-03-27 | 2002-03-27 | |
US10/330,926 US6951566B2 (en) | 2002-01-25 | 2002-12-27 | Reciprocating cutting and dilating balloon |
Publications (2)
Publication Number | Publication Date |
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US20030144677A1 true US20030144677A1 (en) | 2003-07-31 |
US6951566B2 US6951566B2 (en) | 2005-10-04 |
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US10/330,926 Expired - Fee Related US6951566B2 (en) | 2002-01-25 | 2002-12-27 | Reciprocating cutting and dilating balloon |
Country Status (8)
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US (1) | US6951566B2 (en) |
EP (1) | EP1581298B1 (en) |
JP (1) | JP2006512137A (en) |
AT (1) | ATE337044T1 (en) |
AU (1) | AU2003303621A1 (en) |
CA (1) | CA2511544A1 (en) |
DE (1) | DE60307897T2 (en) |
WO (1) | WO2004060467A1 (en) |
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Also Published As
Publication number | Publication date |
---|---|
DE60307897D1 (en) | 2006-10-05 |
DE60307897T2 (en) | 2007-03-08 |
EP1581298A1 (en) | 2005-10-05 |
CA2511544A1 (en) | 2004-07-22 |
JP2006512137A (en) | 2006-04-13 |
US6951566B2 (en) | 2005-10-04 |
WO2004060467A1 (en) | 2004-07-22 |
ATE337044T1 (en) | 2006-09-15 |
AU2003303621A1 (en) | 2004-07-29 |
EP1581298B1 (en) | 2006-08-23 |
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